Business · 26/02/2026Updated: 10/16/2026 · 1 min read

FDA Announces Proposed Collection of Information for Paperwork Reduction Act Review

Summary

The FDA is seeking OMB review and clearance for a proposed collection of information related to Investigational Device Exemptions Reports and Records, as mandated by the Paperwork Reduction Act of 1995.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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